101038-65-7

Basic information

• Product Name: Benzoic acid, 4-(1-piperidinyl)-, ethyl ester
• CAS NO: 101038-65-7
• Molecular Formula: C14H19NO2
• Molecular Weight: 233.31
• Mol File: 101038-65-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(1-piperidinyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(1-piperidinyl)-, ethyl ester(101038-65-7)
• EPA Substance Registry System: Benzoic acid, 4-(1-piperidinyl)-, ethyl ester(101038-65-7)

Safety Data

• Hazardous Substances Data: 101038-65-7(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 5798-75-4 Ethyl 4-bromobenzoate 
• 451-46-7 4-fluorobenzoic acid ethyl ester 
• 2156-71-0 N-chloropiperidine 
• 131379-15-2 (4-(ethoxycarbonyl)phenyl)zinc(ll) bromide 
• 111-24-0 1,5-dibromo-pentane 
• 94-09-7 p-aminoethylbenzoate 

Downstream Products

• 22090-24-0 4-piperidin-1-yl-benzoic acid 
• 106947-71-1 4-(Piperidin-1-yloxy)-benzoic acid ethyl ester 
• 106947-65-3 1-(4-(ethoxycarbonyl)phenyl)piperidine 1-oxide 

Relevant articles and documents

Improved functional group C compatibility in the palladium-catalyzed amination of aryl bromides

Aryl bromides are coupled with amines in the presence of a palladium catalyst and a stoichiometric amount of cesium carbonate. Using these conditions base-sensitive functional groups, which were incompatible with our previously reported catalytic-amination reaction conditions, are well tolerated.

Organic semiconductor photocatalyst can bifunctionalize arenes and heteroarenes

Photoexcited electron-hole pairs on a semiconductor surface can engage in redox reactions with two different substrates. Similar to conventional electrosynthesis, the primary redox intermediates afford only separate oxidized and reduced products or, more rarely, combine to one addition product. Here, we report that a stable organic semiconductor material, mesoporous graphitic carbon nitride (mpg-CN), can act as a visible-light photoredox catalyst to orchestrate oxidative and reductive interfacial electron transfers to two different substrates in a two- or three-component system for direct twofold carbon–hydrogen functionalization of arenes and heteroarenes. The mpg-CN catalyst tolerates reactive radicals and strong nucleophiles, is straightforwardly recoverable by simple centrifugation of reaction mixtures, and is reusable for at least four catalytic transformations with conserved activity.

Pyrazolo [3,4 - the b] pyridine and [...] composition preparation method and use of (by machine translation)

The present invention provides a pyrazolo [3,4 - the b] pyridine and [...] compound of preparation and use, in particular, the present invention provides a following formula (I) compounds are shown, wherein the definition of each group as described in the specification. The compounds of the invention has excellent tyrosine kinase inhibiting activity, so can be used for preparing a series of treating diseases associated with the tyrosine kinase activity of the drug. (by machine translation)